DrugDev Introduces Consent Engineering, the Clinical Trials Industry’s First Truly SaaS Solution for Creating, Managing and Automating Informed Patient Consent In-House

Our mission here is not to do eConsent a little bit better, but to fundamentally change how sponsors and CROs manage consent by giving them the power to build and manage a full consent system.

Today at the 2018 SCOPE Summit for Clinical Operations Executives, DrugDev (an IQVIA company) unveiled the industry’s first truly SaaS solution for electronic patient informed consent. Consent Engineering, the latest addition to the DrugDev Spark™ clinical operations suite, provides all the proven benefits of standard eConsent with the added ability for sponsors and CROs to develop robust and scalable consent systems without having to rely on external providers.

For the first time, Consent Engineering on DrugDev Spark gives study teams the tools, training and best practice resources they need to create, manage and automate consent solutions in-house. This new ability significantly streamlines the time and cost of development and implementation, enabling sponsors and CROs to bring the proven benefits of eConsent to millions more patients worldwide.

eConsent systems already are transforming patient satisfaction and retention, study team efficiency, and regulatory compliance in clinical trials worldwide. DrugDev introduced the life sciences industry to eConsent in 2005 and has since partnered with leading pharmaceutical companies and clinical research organizations (CROs) to implement solutions on over 100 studies.

“Our mission here is not to do eConsent a little bit better, but to fundamentally change how sponsors and CROs manage consent by giving them the power to build and manage a full consent system,” said Eric Delente, President, Patient Consent at DrugDev. “Consistently across companies, consent is one of the most…

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